Download Heart Failure, Second Edition by Marc Semigran, Jordan T. Shin PDF

By Marc Semigran, Jordan T. Shin

Heart Failure, moment Edition has been up-to-date to supply the most recent developments in middle failure examine. Supplemented via greater than two hundred high quality figures and illustrations, the e-book is helping cardiologists and emergency care physicians quick and appropriately establish the reason and severity of a patient’s cardiac impairment.

New subject matters during this version include:

  • Developments in mechanical and pharmacologic remedies
  • Discoveries in developmental biology
  • Up-and-coming imaging modalities
  • Surgical concepts for mechanical circulatory aid and cardiac transplantation
  • Pharmacogenomics and gene-based and cell-based cures
  • Gene expression/recurrence in center failure
  • Changes in metabolic substrate usage and pathways

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Extra info for Heart Failure, Second Edition

Sample text

Bione S, Maestrini E, Rivella S, et al. Identification of a novel X-linked gene responsible for Emery– Dreifuss muscular dystrophy. Nat Genet 1994; 8: 323–7. 52. Hutchison CJ. Lamins: building blocks or regulators of gene expression?. Nat Rev Mol Cell Biol 2002; 3: 848–58. 53. Olson TM, Michels VV, Thibodeau SN, et al. Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science 1998; 280: 750–2. 54. MacRae CA. Genetics and dilated cardiomyopathy: limitations of candidate gene strategies.

Cell 1994; 77: 701–12. 99. Geier C, Perrot A, Ozcelik C, et al. Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy. Circulation 2003; 107: 1390–5. 100. Watkins H, Conner D, Thierfelder L, et al. Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy. Nat Genet 1995; 11: 434–7. 101. Kimura A, Harada H, Park JE, et al. Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy.

46. Olson TM, Keating MT. Mapping a cardiomyopathy locus to chromosome 3p22-p25. J Clin Invest 1996; 97: 528–32. 47. Fatkin D, MacRae C, Sasaki T, et al. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. N Engl J Med 1999; 341: 1715–24. 48. Towbin JA, Hejtmancik JF, Brink P, et al. X-linked dilated cardiomyopathy: molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.

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